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Symbol
Name
ID

Pign
phosphatidylinositol glycan anchor biosynthesis, class N
MGI:1351629

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Hypertelorism	Nystagmus	Amblyopia
Disease(s) Associated with PIGN
multiple congenital anomalies-hypotonia-seizures syndrome 1

Mouse Phenotypes		abnormal eye morphology	coloboma	microphthalmia	abnormal retina morphology	abnormal vitreous body morphology	anophthalmia
Availability	Mouse Genotype	abnormal eye morphology	coloboma	microphthalmia	abnormal retina morphology	abnormal vitreous body morphology	anophthalmia
	Pign^em1(IMPC)Mbp/Pign^em1(IMPC)Mbp
	Pign^m1Nisw/Pign^m1Nisw
	Pign^em1(IMPC)Mbp/Pign⁺

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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